General Electric LC9 Series Basic Service Manual English Version_SM_5482298-100_5 LOGIQ C9 Series Basic Service Manual

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Technical Publication

LOGIQ C9 Series

Basic Service Manual Direction Number: 5482298-100 English

Rev. 5

Product Information

This Manual covers the software version of R1.x.x for LOGIQ C9 Series ultrasound system.

Manufacturer:

GE Medical Systems (China) Co., Ltd. No. 19, Changjiang Road WuXi National Hi-Tech Development Zone Jiangsu, P.R. China 214028 TEL: +86 510 85225888; FAX: +86 510 85226688 www.gehealthcare.com

Revision history

Revision History

Date

Revision

Rev.1 2014/01/09 Initial Release

Rev.2 2014/03/11 Update for transportation box

Rev.3 2016/06/30 Update spare part list

Rev.4 2016/11/18 Update spare part list

Rev.5 2017/08/23 Update spare part list

Pages Revision Pages Revision

Front Rev. 5 Chapter 6 Rev. 5

Front matter Rev. 5 Chapter 7 Rev. 5

TOC Rev. 5 Chapter 8 Rev. 5

(YYYY/MM/DD) Reason for change

List of Effected Pages (LOEP)

Chapter 1 Rev. 5 Chapter 9 Rev. 5

Chapter 2 Rev. 5 Chapter 10 Rev. 5

Chapter 3 Rev. 5 Index Rev. 5

Chapter 4 Rev. 5 Rear Cover Rev. 5

Chapter 5 Rev. 5

Please verify that you are using the latest revision of this document. Information pertaining to this document is maintained on MyWorkshop/ePDM (GE electronic Product Data Management). If you need to know the latest revision, contact your distributor, local GE Sales Representative or in the USA call the GE Ultrasound Clinical Answer Center at 1 800 682 5327 or 1 262 524 5698.

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Important precautions

Translation policy

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Damage in transportation

All packages should be closely examined at time of delivery. If damage is apparent, write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for” by a GE representative or hospital receiving agent. Whether noted or concealed, damage MUST be reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier. A transportation company will not pay a claim for damage if an inspection is not requested within this 14 day period.

Certified electrical contractor statement - For USA Only

All electrical Installations that are preliminary to positioning of the equipment at the site prepared for the equipment shall be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations and testing shall be performed by qualified GE personnel. In performing all electrical work on these products, GE will use its own specially trained field engineers. All of GE’s electrical work on these products will comply with the requirements of the applicable electrical codes.

The purchaser of GE equipment shall only utilize qualified personnel (i.e., GE’s field engineers, personnel of third-party service companies with equivalent training, or licensed electricians) to perform electrical servicing on the equipment.

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Omission and errors

If there are any omissions, errors or suggestions for improving this documentation, contact the GE Global Documentation Group with specific information listing the system type, manual title, part number, revision number, page number and suggestion details.

Mail the

information to:

GE Medical Systems (China) Co., Ltd. No. 19 Changiang Road Wuxi National Hi-Tech Dev. Zone Jiangsu P.R.China 214028

GE employees should use TrackWise to report service documentation issues.

These issues will then be in the internal problem reporting tool and communicated to the writer.

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Service Safety Considerations

WARNING

DANGER DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH,

ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, to reduce the risk of injury.

For a complete review of all safety requirements, refer to Chapter 1 in the Service Manual.

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Legal notes

Trademarks

Copyrights

The contents of this publication may not be copied or duplicated in any form, in whole or in part, without prior written permission of GE.

GE may revise this publication from time to time without written notice.

All products and their name brands are trademarks of their respective holders.

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Translation policy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-2 Damage in transportation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-12 Certified electrical contractor statement - For USA Only - - - - - - - - - - - - i-12 Omission and errors - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-13 Service Safety Considerations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-14 Legal notes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15 Trademarks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15 Copyrights - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - i-15

Table of Contents Chapter 1 — Introduction

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-2

Manual Overview

Contents in this manual - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-3 LOGIQ C9 Series models covered by this manual - - - - - - - - - - - - - - - - 1-5

Important conventions

Conventions used in book - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-6 Standard hazard icons - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-8

Product icons Labels locations Safety considerations

Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12 Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12 Human Safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-12 Mechanical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-15 Electrical safety - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-18

Dangerous procedure warnings Lockout/Tagout (LOTO) requirements Returning probes and repair parts EMC, EMI and ESD

What is EMC? - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-23 CE Compliance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-23 Electrostatic discharge (ESD) prevention - - - - - - - - - - - - - - - - - - - - - 1-24

Customer assistance

Contact information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-25 Phone numbers for Customer Assistance - - - - - - - - - - - - - - - - - - - - - 1-26 System manufacturer - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-26 Authorized Representative- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 1-27

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Chapter 2 — Site Preparations

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-2

General Ultrasound system requirements

Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-3 Ultrasound system environmental requirements- - - - - - - - - - - - - - - - - - 2-3 Electrical requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-6 EMI limitations - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-9 Probes environmental requirements - - - - - - - - - - - - - - - - - - - - - - - - - 2-11 Time and manpower requirements - - - - - - - - - - - - - - - - - - - - - - - - - - 2-11

Facility needs

Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12

- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-12 Purchaser responsibilities - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-13 Required facility needs - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-14 Desirable features- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-15 Minimal floor plan suggestion- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-16 Recommended floor plan suggestion - - - - - - - - - - - - - - - - - - - - - - - - 2-17 Suggested floor plan, Ultrasound system, and EchoPAC PC in same

room - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18

Networking setup requirements - - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-18

Environmental Dangers

Patient Vicinity UL60601-1 (USA) - - - - - - - - - - - - - - - - - - - - - - - - - - - 2-22 Patient Environment IEC60601-1 and ANSI AAMI ES60601-1 - - - - - - 2-23

Chapter 3 — System Setup

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-2

Setup reminders

Average setup time - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3 Setup warnings- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-3

Receiving and unpacking the equipment

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-6 Warnings for receiving and unpacking - - - - - - - - - - - - - - - - - - - - - - - - 3-6 The Tilt indicator - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-7 Receiving the LOGIQ C9 Series - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-7 Unpacking the LOGIQ C9 Series - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-12 Packing the Equipment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-16

Packing materials - recycling information Preparing for setup

Verify customer order - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18 EMI protection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-18

Completing the setup

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19 Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19 System specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-19

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Electrical specifications - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-20 Connections on the I/O Rear Panel - - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Connecting probes - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21 Powering the system - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-21

System Configuration

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-22 Contents in this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-22 LOGIQ C9 Series configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-22

Peripherals Installation

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-23 Furnished materials - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-24 Peripherals Installation Instructions - - - - - - - - - - - - - - - - - - - - - - - - - 3-26

Connectivity setup

Setup the LOGIQ C9 Series for DICOM Communications- - - - - - - - - - 3-34 How to get the LOGIQ C9 Series to recognize another Device on the

Network - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-36

How to Setup and Use a DICOM Image Storage Service - - - - - - - - - - 3-37

Option Setup

Software Option Installation Procedure - - - - - - - - - - - - - - - - - - - - - - - 3-38

Paperwork after setup

Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-40 User’s Manual(s) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-40 Product Locator Installation Card - - - - - - - - - - - - - - - - - - - - - - - - - - - 3-41

Chapter 4 — General Procedures and Functional Checks

Overview

Purpose of this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2 Special Equipment required - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-2

General procedures

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-4 Power ON/Boot Up - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-5 Power off - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-8 LCD Monitor position adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-10 Logging on to LOGIQ C9 Series as “ADM” - - - - - - - - - - - - - - - - - - - - 4-10 Service Key (Dongle, HASP) - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-11 Exit to Windows Desktop from the LOGIQ C9 Series application

software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-13 Removable media - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-15 Archiving and loading presets - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-16 Download/Upload of System Presets via InSite ExC - - - - - - - - - - - - - 4-17 Data Management - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17 Backup - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-17 Installation and Setup Procedure for Peripherals - - - - - - - - - - - - - - - - 4-17 Moving and transporting the LOGIQ C9 Series - - - - - - - - - - - - - - - - - 4-17 Recording important settings and parameters - - - - - - - - - - - - - - - - - - 4-17 Where are the User Manuals and the Service Manual? - - - - - - - - - - - 4-18 How to display or print the PDF files from the Manual CD-ROM? - - - - 4-18

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Cleaning the Tracball - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-19

Functional checks

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21 Contents in this Section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21 Preparation - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-21 Basic Controls - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22 Operator Panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-22 Touch panel - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-23 Probe/Connectors Check- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-24 Peripheral checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25 Pedals - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-25

Power supply test & adjustments

Power Supply Test Procedure - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-26 Power Supply Adjustment - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-26

Application Turnover Check List

Software Configuration Checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - 4-27

Site Log

Chapter 5 — Components and Functions (Theory)

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-2

Block Diagram and Theory

General Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 Top Console- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-3 Block Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-4 Software Diagram - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-6

Power Diagram

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7 AC Power - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-7

Common Service Platform

Introduction - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 5-8

Chapter 6 — Service Adjustments

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-2

LCD Monitor adjustments

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3 Monitor Adjustments - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-3

Touch Panel

Touch Panel Resolution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 6-5

Control Panel adjustment

Chapter 7 — Diagnostics/Troubleshooting

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-2

Gathering Trouble Data

Overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect Vital System Information - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-3 Collect a Trouble Image with Logs - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-4

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Screen Capture

Check and Record the P1 Key Function - - - - - - - - - - - - - - - - - - - - - - - 7-7 Setting the P1 Key to Screen Capture- - - - - - - - - - - - - - - - - - - - - - - - - 7-7 Capturing a Screen - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-8 Reset the P1 Key to Customer’s Functionality - - - - - - - - - - - - - - - - - - 7-10

Common Diagnostics

Utilities- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-11 PC Diagnostics - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-12 PC Diagnostics (Interactive Tests) - - - - - - - - - - - - - - - - - - - - - - - - - - 7-12 Restart LOGIQ C9 Series After Diagnostics - - - - - - - - - - - - - - - - - - - 7-12

Network Configuration

Network Configuration - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 7-13

Chapter 8 — Replacement Procedures

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-2

Warnings and important information

Warnings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-3 Returning/shipping probes and repair parts - - - - - - - - - - - - - - - - - - - - - 8-4

Disassembly/Re-assembly

Warning and Caution - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-5 Tools needed for servicing LOGIQ C9 Series - - - - - - - - - - - - 8-6 Overview of LOGIQ C9 Series - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-7 Body Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-9 Air Filter Cleaning - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-10 Trackball Roller Cleaning- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-12

Loading the software

Purpose of this section - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13 Customer provided prerequisite - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-13 Data Management - moving all images - - - - - - - - - - - - - - - - - - - - - - - 8-13 Backing up the Patient Archive and System Configurations - - - - - - - - 8-14 Recording important settings and parameters - - - - - - - - - - - - - - - - - - 8-14 Loading the System Software - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-15 Option strings - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 8-22

Chapter 9 — Renewal Parts

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-2

List of Abbreviations Renewal Parts Lists

ACDC Power Pack - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4 Operator Console Assy - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-4 Probe - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5 Peripheral - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-5 Power Cord - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7 Manuals- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7 Accessories and Kits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 9-7

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Chapter 10 — Care and Maintenance

Overview

Contents in this chapter - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-2

Warnings Why do maintenance

Periodic maintenance inspections - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4 Keeping records - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-4 Quality assurance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-5

Maintenance task schedule

How often should maintenance tasks be performed? - - - - - - - - - - - - - 10-6

Tools required

Standard GE tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-8 GE-2 tool kit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-10 Special tools, supplies and equipment used for maintenance - - - - - - 10-11

System maintenance

Preliminary checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-12 Functional checks - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-13 Physical inspection - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-15 Optional Diagnostic Checks- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-16 Probe maintenance - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-17

Electrical safety tests

Safety test overview - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-19 Leakage current limits - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-21 Outlet test - wiring arrangement - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-23 Grounding continuity - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-24 Chassis leakage current test - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-25 Probe leakage current test- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-27

When there's too much leakage current …

AC/DC Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30 Chassis Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-30 Probe Fails- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31 Peripheral Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31 Still Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31 New Unit - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31 ECG Fails - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-31

Inspection Paperwork

Ultrasound Inspection Forms - - - - - - - - - - - - - - - - - - - - - - - - - - - - - 10-32

Electrical Safety Tests Log

Index

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Chapter 1

Introduction

This chapter describes important issues related to safely servicing the Ultrasound system. The service provider must read and understand all the information presented here before installing or servicing the units.

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Introduction

Contents in this chapter

• ‘Overview’ on page 1-2

• ‘Manual Overview’ on page 1-3

• ‘Important conventions’ on page 1-6

• ‘Product icons’ on page 1-10

• ‘Labels locations’ on page 1-11

• ‘Safety considerations’ on page 1-12

• ‘Dangerous procedure warnings’ on page 1-20

• ‘Lockout/Tagout (LOTO) requirements’ on page 1-21

• ‘Returning probes and repair parts’ on page 1-22

• ‘EMC, EMI and ESD’ on page 1-23

• ‘Customer assistance’ on page 1-25

Overview

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This manual provides installation and service information for the LOGIQ C9 Series Ultrasound system. It is divided in ten chapters as shown below.

Contents in this manual

The manual is divided into ten chapters.

In the beginning of the manual, before chapter 1, you will find the Revision overview, the Important precautions including

Translation policy, Damage in transportation, Certified electrical contractor statement, Omission & errors, Service safety considerations and Legal notes, and the Table of Contents (TOC).

Manual Overview

Chapter number

An Index has been included after Chapter 10.

Table 1-1: Contents in this manual

Chapter title Description

Introduction Contains a content summary and warnings.

Site preparations Contains pre-setup requirements for the LOGIQ

C9 Series.

System Setup Contains setup procedure with procedure

checklist for the system.

General Procedures and Functional Checks

Components and Functions (Theory)

Service Adjustments Contains instructions on how to make any

Contains functional checks that must be performed as part of the installation, or as required during servicing and periodic maintenance.

Contains block diagrams and functional explanations of the electronics.

available adjustments to the LOGIQ C9 Series.

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Introduction

Table 1-1: Contents in this manual (Continued)

Chapter

Chapter title Description

number

Diagnostics/ Troubleshooting

Replacement procedures

Provides procedures for running diagnostic or related routines for the LOGIQ C9 Series.

Provides disassembly procedures and reassembly procedures for all changeable FRU.

Renewal Parts Contains a complete list of replacement parts for

LOGIQ C9 Series.

10.

Care & Maintenance Provides periodic maintenance procedures for

LOGIQ C9 Series.

N/A Index A quick way to the topic you’re looking for.

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LOGIQ C9 Series models covered by this manual

Table 1-2: LOGIQ C9 Series Model Designations

Model Number Description System SW

5489329 LOGIQ C9 Premium for China R1.x.x

5489330 LOGIQ C9 Expert for China (with 4D) R1.x.x

5489331 LOGIQ C9 Expert for China R1.x.x

5489332 LOGIQ C9 Expert for India R1.x.x

NOTE: When not otherwise specified, the contents of this manual

applies to all LOGIQ C9 Series models.

Manual Overview

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Introduction

Conventions used in book

Important conventions, used in this document, are described next.

Model designations

This manual covers the LOGIQ C9 Series Ultrasound systems listed in:

‘LOGIQ C9 Series models covered by this manual’ on page 1-5.

Icons

Important conventions

Pictures, or icons, are used wherever they will reinforce the printed message. The icons, labels, and conventions used on the product and in the service information are described in this chapter.

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Safety precaution messages

DANGER

WARNING

CAUTION

Various levels of safety precaution messages may be found on the equipment and in the service information. The different levels of concern are identified by a flag word that precedes the precautionary message. Known or potential hazards to personnel are labeled in one of three ways:

• DANGER

• WARNING

• CAUTION

Danger is used to indicate the presence of a hazard that will cause severe personal injury or death if the instructions are ignored.

Warning is used to indicate the presence of a hazard that can cause severe personal injury and property damage if instructions are ignored.

Important conventions

Caution is used to indicate the presence of a hazard that will or can cause minor personal injury and property damage if instructions are ignored. Equipment damage possible.

NOTE: Notes are used to provide important information about an item

or a procedure.

NOTE: Be sure to read the notes; the information contained in a note

can often save you time or effort.

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Introduction

Standard hazard icons

Important information will always be preceded by either the exclamation point (!) contained within a triangle, or the symbols for “Danger”, “Warning” or “Caution”, as seen throughout this chapter. In addition to text, several different graphical icons (symbols) may be used to make you aware of specific types of hazards that could possibly cause harm. Even if a symbol isn’t used in this manual, it may be included for your reference.

Table 1-3: Standard hazard icons

ELECTRICAL

MECHANICAL

RADIATION

LASER

HEAT

PINCH

NOTE: Even if a symbol isn’t used on the product or in this manual, it

may be included for your reference.

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Important conventions

Standard Icons that indicate that a special procedure is to be used

Some others icons make you aware of specific procedures that should be followed.

Table 1-4: Standard Icons that indicates that a special procedure is to be used

Avoid Static Electricity Tag and Lock Out Wear Eye Protection

Hand Protection Foot Protection Wear Eye Protection

Be sure to read the notes; the information contained in a note can often save you time or effort.

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Introduction

Product icons

It is important to refer to the current revision of the Ultrasound system’s User Manual for a full list of product labels prior to servicing the system.

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Labels locations

It is important to refer to the current revision of the Ultrasound system’s User Manual for a full list of product labels prior to servicing the system.

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Introduction

DANGER

WARNING

Contents in this section

• ‘Introduction’ on page 1-12

• ‘Human Safety’ on page 1-12

• ‘Mechanical safety’ on page 1-15

• ‘Electrical safety’ on page 1-18

Introduction

The following safety precautions must be observed during all phases of operation, service and repair of this equipment. Failure to comply with these precautions or with specific warnings elsewhere in this manual, violates safety standards of design, manufacture and intended use of the equipment.

Safety considerations

Human Safety

• Operating personnel must not remove the system covers.

• Servicing should be performed by authorized personnel only.

Only personnel who have participated in a LOGIQ C9 Series Training Seminar are authorized to service the equipment.

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

If the covers are removed from an operating LOGIQ C9 Series, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.

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Human Safety (continued)

WARNING

Because of the limited access to cabinets and equipment in the field, placing people in awkward positions, GE has limited the lifting weight for one person in the field to 16 KG (35 LBS). Anything over 16 KG (35 LBS) requires 2 people.

Have two people available to deliver and unpack the LOGIQ C9 Series.

Attempts to move the Ultrasound system considerable distances or on an incline by one person could result in injury or damage or both.

Explosion Warning

DO NOT operate the equipment in an explosive atmosphere. Operation of any electrical equipment in such an environment constitutes a definite safety hazard.

Safety considerations

DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY install GE approved parts. DO NOT perform any unauthorized modification of the equipment.

Ensure that the Ultrasound system is turned off and unplugged

Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation. The amber light on the OP panel ON/OFF button will turn off.

Ultrasound system components may be energized. Always refer to the Ultrasound system's Proprietary Service Manual for LOTO warnings and cautions

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Introduction

WARNING

Human Safety (continued)

Risk of electrical shock, Ultrasound system must be turned off and disconnected from power source. Cord must be controlled at all times.

Wait for at least 20 seconds for capacitors to discharge as there are no test points to verify isolation. The amber light on the OP panel on/off button will turn off.

Ultrasound System components may be energized. Always refer to the Ultrasound system's Proprietary Service Manual for LOTO warnings and cautions

Use all Personal Protection Equipment (PPE) such as gloves, safety shoes, safety glasses, and kneeling pad, to reduce the risk of injury.

Beware of possible sharp edges on all mechanical parts. If sharp edges are encountered, the appropriate PPE should be used to reduce the risk of injury.

Wear all PPE including gloves as indicated in the chemical MSDS.

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Mechanical safety

WARNING

CAUTION

Safety considerations

While the software install procedure is designed to preserve data, you should save any patient data, images, system setups to removable media or hardcopy before doing a software upgrade.

Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling. Use care when handling and protect from damage when not in use. Do NOT use a damaged or defective probe. Failure to follow these precautions can result in serious injury and equipment damage.

Never use a probe that has fallen to the floor. Even if it looks OK, it may be damaged.

When the Ultrasound system is raised for a repair or moved along any incline, use extreme caution since it may become unstable and tip over.

Take extra care when moving the system.

The LOGIQ C9 Series weighs approximately 130 kg (287 lbs) or more, depending on installed peripherals, when ready for use. To avoid possible injury and equipment damage when transporting from one area of use to another:

• Be sure the pathway is clear.

• Limit movement to a slow careful walk.

• Use two or more persons to move the equipment on inclines or long distance.

Before you move or transport the Ultrasound system, make sure to lock the LCD monitor arm firmly and flip down the monitor to prevent damage to the Ultrasound system.

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Introduction

CAUTION

Mechanical safety (continued)

To avoid injury when you move the LCD monitor and the monitor arm, do not put your finger, hand, or object on the joint of the monitor or the monitor arm.

Ensure that nobody touches the console arm when moving the operator panel.

Do not move the Ultrasound system if the Operator Panel is in unlocked position.

Do not transport LOGIQ C9 Series in a vehicle without locking the casters (wheels) and securing it as described in chapter 4.

Use protective glasses during drilling, filing smooth surfaces, and during all other work where eyes need protection.

Use safety shoes when doing work where there is any chance of foot injury.

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Mechanical safety (continued)

CAUTION

Use protective gloves when working with sharp edges or when directed to wear PPE during a removal/replacement procedure.

Be careful not to pinch any of the cables.

NOTE: Special care should be taken when transporting the Ultrasound

system in a vehicle:

• Before transporting, place the system in its special storage case.

• Lock the wheels (brake)

• Ensure that the system is firmly secured while inside the vehicle.

• Secure system with straps or as directed otherwise to prevent motion during transport.

• Prevent vibration damage by driving cautiously. Avoid unpaved roads, excessive speeds, and erratic stops or starts.

Safety considerations

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Introduction

WARNING

Electrical safety

Safe practices

Follow these guidelines to minimize shock hazards whenever you are using the Ultrasound system:

• To minimize shock hazard, the equipment chassis must be connected to an electrical ground.

• The Ultrasound system is equipped with a three-conductor AC power cable. This must be plugged into an approved electrical outlet with safety ground.

• The power outlet used for this equipment should not be shared with other types of equipment.

• Both the system power cable and the power connector must meet international electrical standards

Connecting a LOGIQ C9 Series to the wrong voltage level will most likely destroy it.

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Probes

Safety considerations

Follow these guidelines before connecting a probe to the Ultrasound system:

• Inspect the probe prior to each use for damage or degradation to the:

• housing

• cable strain relief

• lens

• seal

• connector pins

• locking mechanism

• Do not use a damaged or defective probe.

• Never immerse the probe connector or adapter into any liquid.

• The system has more than one type of probe port. Use the appropriate probe port designed for the probe you are connecting.

Peripherals

Refer to the Patient Safety Environment section of the User’s Manual for peripheral isolation information.

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Introduction

DANGER

WARNING

Dangerous procedure warnings

Warnings, such as the example below, precede potentially dangerous procedures throughout this manual. Instructions contained in the warnings must be followed.

DANGEROUS VOLTAGES, CAPABLE OF CAUSING DEATH, ARE PRESENT IN THIS EQUIPMENT. USE EXTREME CAUTION WHEN HANDLING, TESTING AND ADJUSTING.

If the covers are removed from an operating LOGIQ C9 Series, some metal surfaces may be warm enough to pose a potential heat hazard if touched, even while in shutdown mode.

Explosion Warning

DO NOT operate the equipment in an explosive atmosphere. Operation of any electrical equipment in such an environment constitutes a definite safety hazard.

DO NOT substitute parts or modify equipment

Because of the danger of introducing additional hazards, ONLY install GE approved parts. DO NOT perform any unauthorized modification of the equipment.

SHUT DOWN FORCEDLY OR PLUG IN/OUT ACDC INVALID MAY CAUSE THE DAMAGE OF SYSTEM FILES.

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Lockout/Tagout (LOTO) requirements

WARNING

Lockout/Tagout (LOTO)

requirements

Follow Lockout/Tagout requirements by ensuring you are in total control of the AC power plug at all times during the service process.

To apply Lockout/Tagout (LOTO):

1. Plan and prepare for shutdown.

2. Shutdown the equipment.

3. Isolate the equipment.

4. Remove/disconnect the battery, if present.

5. Apply Lockout/Tagout Devices.

6. Control all stored and residual energy.

7. Verify isolation.

All potentially hazardous stored or residual energy is relieved.

Energy Control and Power Lockout for LOGIQ C9 Series.

When servicing parts of the Ultrasound system where there is exposure to voltage greater than 30 volts:

1. Follow LOCK OUT/TAG OUT procedures.

2. Turn off the breaker.

3. Unplug the Ultrasound system.

4. Maintain control of the Ultrasound system power plug.

5. Wait for at least 30 seconds for capacitors to discharge as there are no test points to verify isolation.

6. Remove/disconnect the battery, if present.

Ultrasound System components may be energized.

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Introduction

Returning probes and repair parts

Equipment being returned must be clean and free of blood and other infectious substances. GE policy states that body fluids must be properly removed from any part or equipment prior to shipment. GE employees, as well as customers, are responsible for ensuring that parts/equipment have been properly decontaminated prior to shipment. Under no circumstance should a part or equipment with visible body fluids be taken or shipped from a clinic or site (for example, body coils or an ultrasound probe).

The purpose of the regulation is to protect employees in the transportation industry, as well as the people who will receive or open this package.

NOTE: The US Department of Transportation (DOT) has ruled that

“items that were saturated and/or dripping with human blood that are now caked with dried blood; or which were used or intended for use in patient care” are “regulated medical waste” for transportation purposes and must be transported as a hazardous material.

NOTE: The USER/SERVICE staff should dispose of all the waste

properly, per federal, state, and local waste disposal regulations.

The Ultrasound system is not meant to be used for long-term storage of patient data or images. The user is responsible for the data on the system and a regular backup is highly recommended.

If the system is sent for repair, please ensure that any patient information is backed up and erased from the system before shipping. It is always possible during system failure and repair to lose patient data. GE is not responsible for the loss of this data.

If PHI (Patient Healthcare Information) data needs to be sent to GE employees for service purposes, GE will ascertain agreement from the customer. Patient information shall only be transferred by approved service processes, tools and devices restricting access, protecting or encrypting data where required, and providing traceability in the form of paper or electronic documents at each stage of the procedure while maintaining compliance with cross-border restrictions of patient information transfers.

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What is EMC?

EMC, EMI and ESD

Electromagnetic compatibility describes a level of performance of a device within its electromagnetic environment. This environment consists of the device itself and its surroundings including other equipment, power sources and persons with which the device must interface. Inadequate compatibility results when a susceptible device fails to perform as intended due interference from its environment or when the device produces unacceptable levels of emission to its environment. This interference is often referred to as radio–frequency or electromagnetic interference (RFI/EMI) and can be radiated through space or conducted over interconnecting power of signal cables. In addition to electromagnetic energy, EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and disturbances in the electrical power supply.

CE Compliance

LOGIQ C9 Series conforms to all applicable conducted and radiated emission limits and to immunity from electrostatic discharge, radiated and conducted RF fields, magnetic fields and power line transient requirements.

For applicable standards, refer to the Safety Chapter of the Ultrasound system’s User’s Manual.

NOTE: For CE Compliance, it is critical that all covers, screws,

shielding, gaskets, mesh, clamps, are in good condition, installed tightly without skew or stress. Proper installation following all comments noted in this service manual is required in order to achieve full EMC performance.

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Introduction

WARNING

Electrostatic discharge (ESD) prevention

DO NOT touch any boards with integrated circuits prior to taking the necessary ESD precautions.

Always connect yourself, via an arm-wrist strap, to the advised ESD connection point located on the rear of the Ultrasound system (near the power connector).

Follow general guidelines for handling of electrostatic sensitive equipment.

Risk of electrical shock, Ultrasound system must be turned off. Avoid all contact with electrical contacts, conductors and components. Always use non-conductive handles designed for the removal and replacement of ESD sensitive parts. All parts that have the potential for storing energy must be discharged or isolated before making contact.

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Contact information

Customer assistance

If this equipment does not work as indicated in this service manual or in the user manual, or if you require additional assistance, please contact the local distributor or appropriate support resource, as listed below.

Before you call, identify the following information, and acquire image (Alt+D) to send to the Customer Care team:

1. System ID serial number.

2. Software version.

3. Date and time of occurrence.

4. Sequence of events leading to issue.

5. Is the issue repeatable?

6. Imaging mode, probe, preset/application.

7. Media brand, speed, capacity, type.

8. Save secondary image capture, cine loop, 4D multi-volume loop.

NOTE: Restart the application before resuming clinical scanning.

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Introduction

Phone numbers for Customer Assistance

Table 1-5: Phone numbers for Customer Assistance

LOCATION PHONE NUMBER

USA GE Healthcare - GE Medical Systems Ultrasound Service Engineering 9900 Innovation Drive Wauwatosa, WI 53226

Canada Phone: 1-800-668-0732

Latin America Service

Europe (OLC-EMEA) GE Ultraschall Deutschland Gmbh & Co. KG Beethovenstraße 239 Postfach 11 05 60, D-42655 Solingen Germany

Online Services Ultrasound Asia Phone:

Service: On-site 1-800-437-1171

Service Parts 1-800-558-2040

Application Support 1-800-682-5327 or

1-262-524-5698

Application Support

OLC - EMEA Phone:

Fax: +49 (0) 2122-8024-31

• Australia

• China

• India

• Japan

• Korea

• Singapore

1-800-321-7937 1-262-524-5698

+49 (0) 212 2802 - 652 +33 1 3083 1300

+(61) 1-800-647-855 +(86) 800-810-8188 +(91) 1800-425-8025 +(81) 42-648-2940 +(82) 2620 13585 +(95) 6277-3444

System manufacturer

Table 1-6: System manufacturer

MANUFACTURER PHONE NUMBER FAX NUMBER

GE Medical Systems (China) Co., Ltd. No.19 Changjiang Road WuXi National Hi-Tech Development Zone Jiangsu P.R.China 214028

+86 510 85225888 +86 510 85226688

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Authorized Representative

Table 1-7: Authorized Representative

AUTHORIZED REPRESENTATIVE

Customer assistance

TELEPHONE / FAX

NUMBER

The location of the CE marking is shown in the Safety chapter of the User manual.

Authorized EU Representative/European registered place of business: GE Medical Systems Information Technologies GmbH (GEMS IT GmbH) Munzinger Strasse 5, D-79111 Freiburg, GERMANY

+49 761 45 43 -0 / +49 761 45 43 -233

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Introduction

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Chapter 2

Site Preparations

This chapter provides the information required to plan and prepare for the setup of an Ultrasound system. Included are descriptions of the facility and electrical needs to be met by the purchaser of the units.

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Site Preparations

Contents in this chapter

• ‘Overview’ on page 2-2

• ‘General Ultrasound system requirements’ on page 2-3

• ‘Facility needs’ on page 2-12

• ‘Environmental Dangers’ on page 2-22

Overview

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General Ultrasound system

CAUTION

Contents in this section

• ‘Ultrasound system environmental requirements’ on

page 2-3

• ‘Electrical requirements’ on page 2-6

• ‘EMI limitations’ on page 2-9

• ‘Probes environmental requirements’ on page 2-11

• ‘Time and manpower requirements’ on page 2-11

General Ultrasound system requirements

requirements

Ultrasound system environmental requirements

If the Ultrasound system is very cold or hot

When unpacking the Ultrasound system, allow the temperature of the Ultrasound system to stabilize before powering up. The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.

If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.

Table 2-1: System Acclimation Time Chart

Degree C 50 45 40 35 30 25 20 15 10 5 0 -5

Degree F 122 113 104 95 86 77 68 59 50 41 32 23

hours 4 2 0 000000246

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Site Preparations

CAUTION

Environmental specifications for Ultrasound system

The system should be operated, stored, or transported within the parameters outlined below. Either its operational environment must be constantly maintained or the unit must be turned off.

Table 2-2: System Environmental Requirements

Operational Storage Transport (<16hrs.)

Temperature 10° - 40°C

50° - 104°F

Humidity 30 - 80%

non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

Ensure that the probe face temperature does not exceed the normal operation temperature range.

The LOGIQ C9 Series system and probe connector is not waterproof. Do not expose the device to water or any kind of liquid.

-5° - 50°C

23° - 122°F

10 - 90% non-condensing

-5° - 50°C

23° - 122°F

10 - 90% non-condensing

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Cooling

Lighting

General Ultrasound system requirements

The cooling requirement for a console Ultrasound system with monitor and on board peripherals, is up to 3800 BTU/h. This figure does not include cooling needed for lights, people, or other equipment in the room.

NOTE: Each person in the room places an additional 300 BTU/h

demand on the cooling system.

Bright light is needed for Ultrasound system installation, updates and repairs. However, operator and patient comfort may be optimized if the room light is subdued and indirect. Therefore a combination lighting system (dim/bright) is recommended. Keep in mind that lighting controls and dimmers can be a source of EMI which could degrade image quality. These controls should be selected to minimize possible interference.

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Site Preparations

Electrical requirements

General requirements

NOTE: GE requires a dedicated power and ground for the proper

operation of its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the Ultrasound system.

Sites with a mains power system with defined Neutral and Live

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.

NOTE: Please note that image artifacts can occur, if at any time within

the facility, the ground from the main facility's incoming power source to the Ultrasound system is only a conduit.

Electrical requirements for the Ultrasound system

In the table below, the electrical specifications for the Ultrasound system includes monitor and on board peripherals.

Table 2-3: Electrical Specifications for LOGIQ C9 Series system

Vol tag e

To le r an c e Power Consumption Frequency

220-240 VAC

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Site circuit breaker

CAUTION

Site power outlets

General Ultrasound system requirements

Power outage may occur. The LOGIQ C9 Series requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you do not have any other equipment operating on the same circuit.

It is recommended that the branch circuit breaker for the Ultrasound system be readily accessible.

POWER OUTAGE MAY OCCURE.

The LOGIQ C9 Series requires a dedicated single branch circuit. To avoid circuit overload and possible loss of critical care equipment, make sure you DO NOT have any other equipment operating on the same circuit.

Unit power plug

A dedicated AC power outlet must be within reach of the Ultrasound system without extension cords. Other outlets adequate for the external peripherals, medical and test equipment needed to support this Ultrasound system must also be present within 1 m (3.2 ft.) of the Ultrasound system. Electrical installation must meet all current local, state, and national electrical codes.

If the Ultrasound system arrives without a power plug, or with the wrong plug, you must contact your GE dealer or the installation engineer must supply what is locally required.

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Site Preparations

Power stability requirement

Table 2-4: Power stability requirement

IEC 61000-4-11

Voltage dips, short interruptions and voltage variations on mains supply

< 5%T (> 95% dip) for

0.5 cycle;

40%T (60% dip) for 5 cycles;

70%T (30% dip) for 25 cycles;

< 5%T (>95% dip) for 5 sec

< 5%T (> 95% dip) for

0.5 cycle;

40%T (60% dip) for 5 cycles;

70%T (30% dip) for 25 cycles;

< 5%T (>95% dip) for 5 sec

Mains power quality should be that of a typical commercial or hospital environment.

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EMI limitations

General Ultrasound system requirements

Ultrasound systems are susceptible to Electromagnetic Interference (EMI) from radio frequencies, magnetic fields, and transients in the air or wiring. They also generate EMI. The Ultrasound system complies with limits as stated on the EMC label. However there is no guarantee that interference will not occur in a particular installation.

Possible EMI sources should be identified before the Ultrasound system is installed.

Electrical and electronic equipment may produce EMI unintentionally as the result of a defect. Some of these sources include:

• medical lasers

• scanners

• cauterizing guns

• computers

• monitors

• fans

• gel warmers

• microwave ovens

• light dimmers

• mobile phones

• in-house wireless phones (DECT phones)

• wireless computer keyboard and mouse

• air conditioning system

• High Frequency (HF) surgery equipment

• general AC/DC adapters

The presence of a broadcast station or broadcast van may also cause interference.

See: ‘EMI prevention/abatement’ on page 2-10 for EMI prevention tips.

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Site Preparations

EMI prevention/abatement

Table 2-5: EMI prevention/abatement

EMI RULE DETAILS

Be aware of Radio Frequency sources

Ground the Ultrasound system

Replace all screws, Radio Frequency gaskets, covers, cores

Replace broken Radio Frequency gaskets

Do not place labels where Radio Frequency gaskets touch metal

Use GE specified harnesses and peripherals

Take care with cellular phones

Properly route peripheral cables

• Keep the Ultrasound system at least 5 meters (15 feet) away from other EMI sources.

• Special shielding may be required to eliminate interference problems caused by high frequency, high powered radio or video broadcast signals.

Poor grounding is the most likely reason an Ultrasound system will have noisy images. Check grounding of the power cord and power outlet.

• After you finish repairing or updating the Ultrasound system, replace all covers and tighten all screws.

• Any cable with an external connection requires a magnet wrap at each end.

• Install all covers. Loose or missing covers or Radio Frequency gaskets allow radio frequencies to interfere with the ultrasound signals.

If more than 20% or a pair of the fingers on an Radio Frequency gasket are broken, replace the gasket. Do not turn on the Ultrasound system until any loose metallic part is removed.

Where applicable, never place a label where Radio Frequency gaskets meet the Ultrasound system. Otherwise, the gap created will permit Radio Frequency leakage. Or, if a label has been found in such a position, move the label.

The interconnect cables are grounded and require ferrite beads and other shielding. Also, cable length, material, and routing are all important; do not change from what is specified.

Cellular phones may transmit a 5 V/m signal; that could cause image artifacts.

Where applicable, do not allow cables to lie across the top of the Card Rack or hang out of the peripheral bays. Loop the excess length for peripheral cables inside the peripheral bays. Attach the monitor cables to the frame.

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General Ultrasound system requirements

CAUTION

Probes environmental requirements

Operation, storage and transport temperatures for probes

Probes should be operated, stored, or transported within the parameters outlined below.

Ensure that the probe face temperature does not exceed the normal operation temperature range.

Table 2-6: Probe Environmental Requirements

Operational Storage Transport

Temperature 10° - 40° C

50° - 104° F

Humidity 5 - 85%

non-condensing

Pressure 700 - 1060hPa 700 - 1060hPa 700 - 1060hPa

0° - 55° C 32° - 131° F

5 - 85% non-condensing

-40° - 55° C

-40° - 131° F

5 - 85% non-condensing

Check the room temperature before you use the probe.

Ensure that the probe face temperature does not exceed the normal operation temperature range.

NOTE: Refer to Table 2-1 on page 2-3 to determine the needed

settlement time.

Time and manpower requirements

Site preparation takes time. Begin site preparation checks as soon as possible, if possible, six weeks before delivery, to allow enough time to make any changes.

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Site Preparations

Contents in this section

• ‘Purchaser responsibilities’ on page 2-13

• ‘Required facility needs’ on page 2-14

• ‘Desirable features’ on page 2-15

• ‘Minimal floor plan suggestion’ on page 2-16

• ‘Recommended floor plan suggestion’ on page 2-17

• ‘Suggested floor plan, Ultrasound system, and EchoPAC PC

in same room’ on page 2-18

• ‘Networking setup requirements’ on page 2-18

Facility needs

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Purchaser responsibilities

The work and materials needed to prepare the site is the responsibility of the purchaser. Delay, confusion, and waste of manpower can be avoided by completing pre-installation work before delivery. Purchaser responsibility includes:

• Procuring the materials required

• Completing the preparations before delivery of the Ultrasound system

• Paying the costs for any alterations and modifications not specifically provided in the sales contract

NOTE: All electrical installations that are preliminary to the positioning

of the equipment at the site prepared for the equipment must be performed by licensed electrical contractors. Other connections between pieces of electrical equipment, calibrations, and testing must also be performed by qualified personnel. The products involved (and the accompanying electrical installations) are highly sophisticated and special engineering competence is required. All electrical work on these products must comply with the requirements of applicable electrical codes. The purchaser of GE equipment must only utilize qualified personnel to perform electrical servicing on the equipment.

Facility needs

The desire to use a non–listed or customer provided product or to place an approved product further from the Ultrasound system than the interface kit allows, presents challenges to the installation team. To avoid delays during installation, such variances should be made known to the individuals or group performing the installation at the earliest possible date (preferably prior to the purchase).

The ultrasound suite must be clean prior to delivery of the Ultrasound system. Carpet is not recommended because it collects dust and creates static. Potential sources of EMI (electromagnetic interference) should also be investigated before delivery. Dirt, static, and EMI can negatively impact Ultrasound system reliability.

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Site Preparations

Required facility needs

NOTE: GE requires a dedicated power and ground for the proper

operation of its Ultrasound equipment. This dedicated power shall originate at the last distribution panel before the Ultrasound system.

Sites with a mains power system with defined Neutral and Live

The dedicated line shall consist of one phase, a neutral (not shared with any other circuit), and a full size ground wire from the distribution panel to the Ultrasound outlet.

Sites with a mains power system without a defined Neutral

The dedicated line shall consist of one phase (two lines), not shared with any other circuit, and a full size ground wire from the distribution panel to the Ultrasound outlet.

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Required facility needs (continued)

NOTE: Please note that image artifacts can occur, if at any time within

the facility, the ground from the main facility's incoming power source to the Ultrasound unit is only a conduit.

• Dedicated single branch power outlet of adequate amperage meeting all local and national codes which is located less than 2.5 m (8 ft.) from the unit’s proposed location

• Door opening is at least 76 cm (30 in) wide

• Proposed location for unit is at least 0.5m (1.5 ft.) from the wall for cooling

• Power outlet and place for any external peripheral are within 2 m (6.5 ft.) of each other with peripheral within 1 m of the unit to connect cables.

• Power outlets for other medical equipment.

• Power outlets for test equipment within 1 m (3.2 ft.) of Ultrsound system.

• Clean and protected space to store probes (in their cases or on a rack)

• Material to safely clean probes (done with a plastic container, never metal)

Facility needs

Desirable features

For the amperage requirements, see: ‘Electrical requirements’ on page 2-6.

• Door is at least 92 cm (3 ft.) wide

• Circuit breaker for dedicated power outlet is easily accessible

• Sink with hot and cold water

• Receptacle for bio–hazardous waste, like used probe sheaths

• Emergency oxygen supply

• Storage for linens and equipment

• Nearby waiting room, lavatory, and dressing room

• Dual level lighting (bright and dim)

• Lockable cabinet ordered by GE for its software and proprietary manuals

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Site Preparations

Minimal floor plan suggestion

CSI 8x10

Scale: Each square equals one square foot (app. 31 x 31 cm)

1. Door – at least 762 mm (30 inches)

2. Film Viewer

3. Counter Top, Sink with hot and cold water and Supplies Storage

4. Linen Supply

5. Probes/Supplies

6. Examination Table – 1930 x 610 mm (76 x 24 inches)

7. Footswitch

8. Stool

9. Ultrasound system

10. External Peripherals

11. Dedicated Power Outlet Circuit Breaker protected and easily accessible

12. Network Interface

13. 457 mm (18 inches) distance of Ultrasound system from wall or objects

14. GE Cabinet for Software and Manuals

Figure 2-1. Minimal floor plan, 2.5 m x 3 m (8 by 10 foot)

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Recommended floor plan suggestion

CSI 14x17

Facility needs

13 14

Scale: Each square equals one square foot (app. 31 x 31 cm)

1. Secretaries or Doctors Desk

2. File Cabinet

3. Film Viewer

4. Counter Top

5. Counter Top and Sink with hot and cold water

6. Overhead Lights Dimmer Dual Level Lighting (bright and dim)

7. Emergency Oxygen

8. Suction Line

9. Ultrasound system

10. Dedicated Power Outlet Circuit Breaker protected and easily accessible

11. Network Interface

12. 457 mm (18 inches) distance of Ultrasound system from wall or objects

13. Stool

14. Footswitch

15. Storage for Linens and Equipment

16. Examination Table – 1930 x 610 mm (76 x 24 inches)

17. Lavatory and Dressing Room

18. Door – at least 762 mm (30 inches)

Figure 2-2. A 14 by 17 foot recommended floor plan

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Site Preparations

Suggested floor plan, Ultrasound system, and EchoPAC PC in same

room

1. EchoPAC PC workstation parts

2. UPS

3. Ethernet network wall outlet

4. 3x mains power outlets

5. Hot and Cold water

6. Dedicated mains power outlet

7. Ethernet network wall outlet

Figure 2-3. Suggested Room with EchoPAC PC workstation and Ultrasound Scanner

Networking setup requirements

Stand alone Ultrasound system (without network connection)

None.

Scanner connected to hospital’s network

Supported networks:

10/100 Mbit Ethernet/DICOM network (option)

InSite requirements

InSite requires an Ethernet connection via:

• 10/100 Mbit Interface

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Purpose of the DICOM network function

DICOM services provide the operator with clinically useful features for moving images and patient information over a hospital network.

Examples of DICOM services include the transfer of images to workstations for viewing or transferring images to remote printers.

As an added benefit, transferring images in this manner frees up the on-board monitor and peripherals, enabling viewing to be done while scanning continues.

With DICOM, images can be archived, stored, and retrieved faster, easier, and at a lower cost.

Facility needs

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Site Preparations

DICOM option setup requirements

To configure the Ultrasound system to work with other network connections, the site’s network administrator must provide information to complete the form “Worksheet for DICOM Network Information”. Ensure that there are no spaces in any field of the form.

See:

Entries must include:

• A host name, local port number, AE Title, IP address and Net Mask for the Ultrasound system.

• The IP addresses for the default gateway and other routers at the site for ROUTING INFORMATION.

• The host name, IP address, port and AE Title for each device the site wants connected to the Ultrasound system for DICOM APPLICATION INFORMATION. A field for the make (manufacturer) and the revision of the device, is also included. This information may be useful for error solving.

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DICOM option setup requirements (continued)

Facility needs

Figure 2-4. Worksheet for DICOM Network Information

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Site Preparations

Environmental Dangers

Commercial devices such as laser cameras, printers, VCRs and external monitors, usually exceed allowable leakage current limits and, when plugged into separate AC outlets, are in violation of patient safety standards. Suitable electrical isolation of such external AC outlets, or providing the device with extra protective earth, will be required in order to meet UL60601-1 and IEC60601-1 / IEC60601-1-1 standards for electrical leakage.

Patient Vicinity UL60601-1 (USA)

2.12.20DV (UL60601-1:2003)

In area in which patients are normally cared for, the patient vicinity is the space with surfaces likely to be contacted by the patient or attendant who can touch the patient. This encloses a space within the room 1.83 m (6 ft.) beyond the perimeter of the bed (examination table, dental chair, treatment booth, and the like) in its intended location, and extending vertically 2.29 m (7.5 ft.) above the floor.

1. Patient environment

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Environmental Dangers

Patient Environment IEC60601-1 and ANSI AAMI ES60601-1

Sub Clause 3.79 and figure A.9 (IEC60601-1:2005 and ANSI AAMI ES60601-1:2005)

Such an area is an environment in which medical diagnosis, monitoring or treatment is carried out. It is very difficult to attach unique dimensions to the PATIENT ENVIROMENT.

In practice a distance of 2,5 m (8.2 ft.) above the floor on which the medical personnel stand and a horizontal distance of 1,5 m (4.9 ft.) have justified themselves as indicative of the dimensions of the Patient Environment.

The patient environment/vicinity will be depicted as a dashed line in this procedure. See example below.

1. Patient environment

Figure 2-5. Patient environment

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Site Preparations

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Chapter 3

System Setup

This chapter contains information needed to install LOGIQ C9 Series system.

Included is a procedure that describes how to receive and unpack the equipment and how to file a damage or loss claim.

How to prepare the facility and unit of the actual installation, and how to check and test the unit, probes, and external peripherals for electrical safety are also included in this procedure.

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System Setup

Contents in this chapter

• ‘Overview’ on page 3-2

• ‘Setup reminders’ on page 3-3

• ‘Receiving and unpacking the equipment’ on page 3-6

• ‘Preparing for setup’ on page 3-18

• ‘Completing the setup’ on page 3-19

• ‘System Configuration’ on page 3-22

• ‘Peripherals Installation Instructions’ on page 3-26

• ‘Connectivity setup’ on page 3-34

• ‘Paperwork after setup’ on page 3-40

Overview

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Average setup time

DANGER

CAUTION

Setup warnings

Setup reminders

• Unpacking the LOGIQ C9 Series: 30 minutes

• Set up LOGIQ C9 Series wo/options: 30 minutes

• DICOM Network Configuration: 30 minutes or more, depending on the configuration

• Install Insite: 0.5 hour

The LOGIQ C9 Series installation and functional checkout will take approximately 1 hour. LOGIQ C9 Series consoles with optional equipment may take slightly longer.

WHEN USING ANY TEST INSTRUMENT THAT IS CAPABLE OF OPENING THE AC GROUND LINE (I.E., METER’S GROUND SWITCH IS OPEN), DON’T TOUCH THE ULTRASOUND SYSTEM!

To prevent electrical shock, connect the unit to a properly grounded power outlet. DO NOT use a three to two prong adapter. This defeats safety grounding.

DO NOT wear the ESD wrist strap when you work on live circuits and more than 30 V peak is present.

DO NOT operate this unit unless all board covers and frame panels are securely in place. System performance and cooling require this.

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System Setup

DANGER

CAUTION

Setup warnings (continued)

1. There are no operator serviceable components. To prevent shock, do not remove any covers or panels. Should problems or malfunctions occur, unplug the power cord. Only qualified service personnel should carry out servicing.

NOTE: For information regarding packing labels, refer to LABELS

ON PACKAGE.

2. After being transported, the unit may be very cold or hot. If this is the case, allow the unit to acclimate before you turn it on. It requires one hour for each 2.5°C increment it's temperature is below 10°C or above 40°C.

Equipment damage possibility. Turning the system on without acclimation after arriving at site may cause the system to be damaged.

If the Ultrasound system is very cold or hot, do not turn on its power until it has had a chance to acclimate to its operating environment.

The following table describes guidelines for reaching operational temperatures from storage or transport temperatures.

Table 3-1: System Acclimation Time Chart

Degree C 50 45 40 35 30 25 20 15 10 5 0 -5

Degree F 122 113 104 95 86 77 68 59 50 41 32 23

hours 4 2 0 000000246

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Setup warnings (continued)

CAUTION

Operator Manual(s)

The User Manual(s) should be fully read and understood before operating the LOGIQ C9 Series and kept near the Ultrasound system for quick reference.

Acoustic Output Hazard

Although the ultrasound energy transmitted from the LOGIQ C9 Series probe is within AIUM/NEMA standards, avoid unnecessary exposure. ultrasound energy can produce heat and mechanical damage.

Setup reminders

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System Setup

CAUTION

Receiving and unpacking the

Purpose of this section

This section describes how to receive and unpack LOGIQ C9 Series.

Contents in this section

• ‘Warnings for receiving and unpacking’ on page 3-6

• ‘The Tilt indicator’ on page 3-7

• ‘Receiving the LOGIQ C9 Series’ on page 3-7

• ‘Unpacking the LOGIQ C9 Series’ on page 3-12

equipment

Warnings for receiving and unpacking

GENERIC CRT VERSION

Two people are needed to unpack the Ultrasound system because of its weight. Attempts to move the Ultrasound system considerable distances or on an incline by one person could result in injury or damage or both.

Two people are required whenever a part weighing 16 KG (35 LBS) or more must be lifted.

Remember to use relevant personal protecting equipment (PPE) during packing and unpacking. Check with your local EHS representative.

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Receiving and unpacking the equipment

The Tilt indicator

Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

To make it easier to detect if the handling during transportation has been improper, a set of Tilt indicator has been attached to the transportation box.

Table 3-2: Tilt Watch

Description Illustration

Tilt Watch

Receiving the LOGIQ C9 Series

Overview

Improper handling during transportation may harm the equipment inside the package even if the package itself is undamaged.

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System Setup

Examine all packages

Examine package closely at time of delivery, as described in the procedure below.

Table 3-3: Examine all packages

Step Task Illustrations

1. Is damage apparent?

• If YES; continue with the instructions in ‘Damage in transportation’ on page 3-11.

• If NO; continue with the next step.

2. Is the Tilt Indicator red colored inside the middle of the indicator?

• If YES: The Tilt Indicator has been

activated. Continue with the instructions in ‘Damage in transportation’ on page 3-11 before you continue with the next step.

• If NO: continue with the next step.

3. Continue with the instructions in ‘Unpacking the LOGIQ C9 Series’ on page 3-12.

1 - Red Color

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Position of the Tilt indicator

The Tilt indicator has been attached to the transportation box as illustrated in the figure below.

Receiving and unpacking the equipment

Figure 3-1. Tilt indicator

1. Tilt Indicator

NOTE: Before cutting the straps, check Tilt Tags to make sure it has not

been triggered. If damaged, report it to the carrier. If not, then cut the straps around the crate.

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System Setup

If Tilt Indicator has triggered or is missing

The purpose of the tilt indicator label is to alert people handling a product that it is sensitive to tipping and it must remain upright at all times. It is basically an active "Up Arrow" that changes color if the package is tipped 89 degrees or more from horizontal. These labels can be false activated if tipped less than 89 degrees, and shocked or vibrated at the same time. This event does occur, but is considered uncommon. If a package is received with an activated tilt indicator label, there is high degree of certainty it tipped 89 degrees or more from horizontal during shipment.

An activated tilt indicator label does not indicate if the package was simply “Tipped” (laid down with no impact shock) or “Tipped Over” (free fall, with an impact shock). Using both shock indicator labels and tilt indicator labels will help identify if a Tip Over impact shock occurred.

Table 3-4: Tilt Indicator has triggered or is missing

Step Task

If the Tilt Indicator is missing:

Note on the shipping papers at the time of receipt that the Tilt Indicator label is missing.

If the Tilt Indicator has triggered:

Note on the shipping papers at the time of receipt that the Tilt Indicator label was activated.

Inspect the product for possible concealed damage.

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Receiving and unpacking the equipment

Damage in transportation

Follow this procedure if damage is apparent:

1. Write “Damage In Shipment” on ALL copies of the freight or express bill BEFORE delivery is accepted or “signed for“ by a GE representative or hospital receiving agent.

2. Report the damage to the carrier.

• Whether noted or concealed, damage MUST be

reported to the carrier immediately upon discovery, or in any event, within 14 days after receipt, and the contents and containers held for inspection by the carrier.

• A transportation company will not pay a claim for

damage if an inspection is not requested within this 14 day period.

LOGIQ C9 Series transportation box label

The LOGIQ C9 Series transportation box label is located at the front of the transportation box.

Figure 3-2. LOGIQ C9 Series transportation box label 1

Figure 3-3. LOGIQ C9 Series transportation box label 2

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System Setup

CAUTION

Unpacking the LOGIQ C9 Series

When a new system arrives, check that any components are not damaged and are not in short supply. If shipping damage or shortage occurs, contact the address shown in Chapter 1.

Please carefully unpack the system, and do not dispose the package of LOGIQ C9 Series, so that it can be reused for service.

Table 3-5: Unpacking the LOGIQ C9 Series

Step Description Corresponding Graphic

1 Tear the stop open mark.

2 Cut the two packing straps around the crate.

Note: To avoid injury, with one hand holding the strap clasp when cutting the strap.

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Receiving and unpacking the equipment

Table 3-5: Unpacking the LOGIQ C9 Series

Step Description Corresponding Graphic

3 Remove the top cover.

4 Open the four plastic locks.

Note: Rotate the inside plastic lock counterclockwise to remove it and then remove the outside lock.

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System Setup

Table 3-5: Unpacking the LOGIQ C9 Series

Step Description Corresponding Graphic

5 Remove the outside shipping box.

6 Remove the dust bag from the unit and remove

the foam in the front of the control panel.

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Receiving and unpacking the equipment

Table 3-5: Unpacking the LOGIQ C9 Series

Step Description Corresponding Graphic

7 Remove the clear plastic (wrapped around the

LOGIQ C9 Series) from the unit.

Note: To avoid damaging the unit, please use a pair of scissors instead of the knife.

8 Remove the foams between the LCD and

control panel.

9 Loosen the tie-down strap. Push the brass

piece to pull back handle, then loosen the strap.

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System Setup

Table 3-5: Unpacking the LOGIQ C9 Series

Step Description Corresponding Graphic

10 Remove the wooden ramp and attach it to the

Pallet base on the rear side of the LOGIQ C9 Series.

11 Pull the LOGIQ C9 Series down the Pallet base

ramp.

Note: Remember to pull the LOGIQ C9 Series from the back for safer transportation.

12 Remove all the covers and foams from the unit.

13 Place all of the filling inside the Transportation

Box. Close the box, and store the filling for possible future use.

Moving into Position

Please refer to User Manual on how to move the system.

Packing the Equipment

Please pack LOGIQ C9 Series in the reverse order of unpacking.

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Packing materials - recycling information

Packing materials - recycling

information

The packing materials for LOGIQ C9 Series are recyclable:

• The Transportation Box is made of spruce or similar material. (“PHYTOSANITARY CERTIFICATE” included in all shipments to The People's Republic of China.)

• Lever lockings (hinges) are made of zinc plated steel.

• The inner reinforcements are made of Ethafoam (Polyethylene foam).

• The plastic foil is made of LDPE (Low Density Polyethylene).

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System Setup

Verify customer order

Compare items received by the customer to that which is listed on the delivery order. Report any items that are missing, back ordered, or damaged.

Physical inspection

Verify that the system arrived intact (visual inspection).

If the system has been damaged, please refer to ‘Damage in transportation’ on page i-12 in the beginning of this manual.

Preparing for setup

EMI protection

The LOGIQ C9 Series has been designed to minimize the effects of Electro-Magnetic Interference (EMI). Many of the covers, shields, and screws are provided primarily to protect the system from image artifacts caused by this interference. For this reason, it is imperative that all covers and hardware are installed and secured before the unit is put into operation.

See ‘EMI limitations’ on page 2-9 for more information about EMI protection.

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Purpose of this section

This section describes how to complete the installation of LOGIQ C9 Series.

Contents in this section

• ‘System specifications’ on page 3-19

• ‘Electrical specifications’ on page 3-20

• ‘Connections on the I/O Rear Panel’ on page 3-21

• ‘Connecting probes’ on page 3-21

• ‘Powering the system’ on page 3-21

Completing the setup

System specifications

System requirements verification

• Verify that the site meets the requirements listed in Chapter 2.

(See: ‘Facility needs’ on page 2-12.)

• Verify that the specifications below don’t conflict with any on-site conditions.

Physical dimensions

Table 3-6: Physical dimensions of LOGIQ C9 Series

Height Width Depth Depth

1250 700 900

49.12 27.56 35.43

Console Weight

• Weight: approx. 130 kg (287 lbs)

Inches

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System Setup

WARNING

Electrical specifications

Connecting a LOGIQ C9 Series to the wrong voltage level will most likely destroy it.

Verification of the system’s voltage setting

Verify that the mains voltage specified for the LOGIQ C9 Series is available on-site.

The voltage setting for the unit is found on a label near the Mains Power Circuit Breaker on the rear of the system.

Refer to the latest revision User Manual for a fill list of product labels.

Electrical specifications for LOGIQ C9 Series

In the table below, the electrical specifications for LOGIQ C9 Series includes monitor and on board peripherals.

Table 3-7: Electrical specifications for LOGIQ C9 Series

Part

Number

5489329 LOGIQ C9 Premium for

5489330 LOGIQ C9 Expert for

5489331 LOGIQ C9 Expert for

5489332 LOGIQ C9 Expert for

Description Volta ge Tolerances

China

China (with 4D)

China

India

Power

consumntion

220-240V ±10% Max.950VA 50/60 Hz

Frequency

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Connections on the I/O Rear Panel

NOTE: Accessory equipment connected to the analog and digital

interfaces must be certified according to the respective IEC standards (e.g. IEC60950 for data processing equipment and IEC60601-1 for medical equipment). Furthermore, all complete configurations shall comply with the valid version of the system standard IEC60601-1. Everybody who connects additional equipment to the signal input part or signal output part of LOGIQ C9 Series, configures a medical system, and is therefore responsible that the Ultrasound system complies with the requirements of the valid version of IEC60601-1. If in doubt, consult the technical service department or your local representative for GE Healthcare.

Connect Ethernet

Connect the network cable to the Ethernet connector on the I/O Rear Panel.

The connector is located on the rear side of LOGIQ C9 Series.

Completing the setup

Connect USB Flash Drive

NOTE: USB Flash Drive approved for LOGIQ C9 Series are verified for

EMC performance according to EN55011 class B. The use of any other USB Flash Drive will compromise this verification, and may cause interference on LOGIQ C9 Series itself, or on other electronic devices.

For approved models, please refer to Chapter 9.

Insert the USB Flash Drive in one of the USB ports on the LOGIQ C9 Series.

Connecting probes

Please refer to User Manual on how to connect/disconnect a probe.

Powering the system

Please refer to User Manual on how to power the system.

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System Setup

System Configuration

Purpose of this section

This section describes how to configure the LOGIQ C9 Series.

Contents in this section

LOGIQ C9 Series configuration

For complete instructions, refer to the lastest revision of the LOGIQ C9 Series Basic User Manual, Chapter 16.

Information includes Entering Location, Adjusting Date and Time, Selecting User interface Language, Selecting Online Manual Language, Slelecting Unites of Measure.

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Overview

Peripherals Installation

This section describes how to install and configure the peripherals validated for the LOGIQ C9 Series.

For LOGIQ C9 Series peripheral list, please refer to ‘Peripheral’ on page 9-5 .

About the operation check-out of peripherals, See ‘Peripheral checks’ on page 4-25 for more information.

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System Setup

Furnished materials

Item Description Quantity Note

1 Sony UP-D897 MD Printer 1

2 Paper Roll 1

3 USB cable 1

Table 3-9: Materials furnished with Color USB Printer

Item Description Quantity Note

This section describes the materials furnished with the Peripherals and with the system.

Retain the original carton and packing materials in case transport is needed in the future.

• B/W USB Printer

Table 3-8: Materials furnished with B/W Printer

• Color USB Printer

1 Sony UP-D25MD Printer 1

2 Paper Roll 1

3 AC Power Cord (local purchase) 1

4 USB cable 1

• Digital Printer

Table 3-10: Materials furnished with B/W Printer

Item Description Quantity Note

1 HP Officejet 100 Printer 1

2 Paper Roll 1

3 USB cable 1

• USB Stick

Table 3-11: Materials furnished with B/W Printer

Item Description Quantity Note

1 SanDisk USB Stick 1

2 Paper Roll 1

3 USB cable 1

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General Electric LC9 Series Basic Service Manual English Version_SM_5482298-100_5 LOGIQ C9 Series Basic Service Manual

Specifications and Main Features

Frequently Asked Questions

User Manual

LOGIQ C9 Series

Table of Contents

Introduction

Overview

Manual Overview

Important conventions

Product icons

Labels locations

Safety considerations

Dangerous procedure warnings

Lockout/Tagout (LOTO) requirements

Returning probes and repair parts

EMC, EMI and ESD

Customer assistance

Site Preparations

Overview

General Ultrasound system requirements

Facility needs

Environmental Dangers

System Setup

Overview

Setup reminders

Packing materials - recycling information

Preparing for setup

Completing the setup

System Configuration

Peripherals Installation